ORPHA:2775
Autosomal recessive carpotarsal osteolysis
inactive · moved to ORPHA:371428Multicentric osteolysis-nodulosis-arthropathy spectrum
Synonyms: Hereditary multicentric osteolysis
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Multicentric osteolysis-nodulosis-arthropathy spectrum
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autosomal recessive carpotarsal osteolysis | Hereditary multicentric osteolysis |
| fr | Ostéolyse carpotarsienne autosomique récessive | Ostéolyse multicentrique |
| de | Osteolyse, karpotarsale, autosomal-rezessive | Osteolyse, hereditäre multizentrische |
| es | Osteólisis carpotarsiana autosómica recesiva | Osteólisis multicéntrica hereditaria |
| it | Osteolisi carpotarsale autosomica recessiva | Osteolisi multicentrica ereditaria |
| nl | Autosomaal recessieve carpotarsale osteolyse | Erfelijke multicentrische osteolyse |
| pt | Osteólise carpo-társica autossómica recessiva | Osteólise multicêntrica hereditária |
| pl | Autosomalna recesywna osteoliza nadgarstkowo-stępowa | Dziedziczna osteoliza wielocentryczna |
| cs | Autozomálně recesivní karpotarzální osteolýza | Dědičná multicentrická osteolýza |
| uk | Аутосомно-рецесивний карпотарзальний остеоліз | Спадковий мультицентровий остеоліз |
| zh | 常染色体隐性腕跗骨骨质溶解 | 遗传性多中心性骨质溶解 |
| tr | Otozomal resesif karpotarsal osteoliz | Kalıtsal çok merkezli osteoliz |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2775
- This record as JSON: /data/d/2775.json